| Tag | Content |
|---|
EnhancerAtlas ID | HS133-11281 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:31008900-31011260 |
Target genes | | Number: 51 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr16:31009373-31009387 | TTTCCCAGGGGAAT | - | 6.32 | | EWSR1-FLI1 | MA0149.1 | chr16:31009098-31009116 | CGAAGGCAGGCAGGAAGG | + | 6.9 | | Esrra | MA0592.2 | chr16:31010139-31010150 | TTCAAGGTCAA | + | 6.14 | | Nr5a2 | MA0505.1 | chr16:31010136-31010151 | GTGTTCAAGGTCAAG | + | 6.13 | | RREB1 | MA0073.1 | chr16:31010370-31010390 | CCACCCCCCACCCCCAAAAC | + | 6.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 31010023 | 31010600 | | chr16 | 31010421 | 31011035 | | chr16 | 31010600 | 31010999 |
|
Enhancer Sequence | GGGAGAGAGG GCGCAGCGAT GGGCGGGAGA CCCGGGGCAC ATGGGGCGAG GGTCCGGGGC 60
GTACGAATGG TCAACACCCC GCGGCAGCGC CAGGCCCGGG GAGAAACGTC ATCCCCAGGG 120
CGAGTTGCGG GCAGCGGTGC CCCAGGGTGG TGTTAGGAGC CAGCAGATAA ACAGACGAAC 180
AGACGTTTGA GGGGGTTCCG AAGGCAGGCA GGAAGGGATA CTGAGGGTCA GAGGGTCACC 240
AGACAGAAGG GGGCTATTTG TTCTAGTGGC AGAACTGGGT CTTGGAAAGT CCCATCAGTG 300
GTAATTCCTG TCCAACTCCA TGAGGGCGTG CCGGCCCAGC CCGCGTGAAG GGGCCATGTA 360
TGTGGGGTGC TCCCTACTTC CTACAGCCTC TGGACAGGGG GCAAGAACAC AGCCTGCCTT 420
TTTTCTGATG GAAGGCAGTC ACCTCCAGGT GGATCAGGTT CTAGTGGCCC CTCTTTCCCA 480
GGGGAATTCA AGGGCAAACA CATGGATATT CCAAGGGAGA AAGCAGCCCT CTCCCTGCCC 540
TGTAAGGTGA TCCCCGATCC GGGAATTCCC ACTTCTGAAG GACGTTCTGG AAAAGTGCAC 600
AGATTAACTG AGATTCCTGC TTCTGGATCA AGCACTCCTG ACACTATCGT TCCGATTTTC 660
TAAAAAAGAG ATTGTGGCAA AATCTACCTC GGTGAGATCA GAAAATGCAG CAGGGATGAA 720
TCACCGGCCC TCTCAGACCT CACCAGCCTC CAGGCCATTC CTAAGAGCCT CACTCCTCCG 780
TTCTGTTGGC AGTGGGGGAG GTACGGGGCC GGATGGCACC CCAAGGCTCC CCCGATTGAG 840
TGACAGCTCT GGCTCAGCAA CACATGGCCC AGGGATATTG GAATCGGCTG GCCCAGATTG 900
GGGCCCGACT GTCAGCCTTG GGGCTGGGGT CAAGTCCGGA GGGAGGGGTC TCTTACAGGA 960
TCTCATTGAC TTTTTACAAC ATTCCTGGGA GTTCAGTGAT ATCAGCTCAT GTTTTAGACT 1020
AGAAACTCAG TTTCCAGTGG GCAAAACCAC TCACTCAAGG TCACACCCAA AGCCTGAGCT 1080
CATGCCACCA GCTGGAAGAG GACTAAGAGA ATCCTCTCTC CTTTCCTGGA GGTCTGAAAG 1140
GTCAGCTTCT CTAAACCACG GCCACTTTTC CAGCTTCTTT CTTGGTCTAT TCCTGAACCC 1200
CTCACCCACA GAGCCCTCCC CAGGGTCTTA CAGAGAGTGT TCAAGGTCAA GGCTTGATGG 1260
ACCTAGAGAA ACCATTGAGC CCAGGGGATT TTAAACTGCC AGCAGGAACC TTGTTTCTGA 1320
GAAGGAATTT CAGGGGCTGT TGCAGAGAAT GAAGAGAGGT CAGGCAGGTA GGTGCTCCCA 1380
GCTCCAGCTC AGCTAGAACA ACCTGACTTT TATGTTTTAT ATATTGGGAT TCTTTGTATG 1440
ACTTTGGAAA AAAAAGTATT TTGATGCCCT CCACCCCCCA CCCCCAAAAC AAGCTAATTT 1500
TGAAATTGCT TTCATTTGTC TTACTGTACT GATAAGGAAG CTGAGAGTAG GGGACTTGTC 1560
CAGGGTGAGC TGATGGTGGA GGTTAGACTC TGTCTGCCTG GATTTGCACT TAACATGCTC 1620
CCAGATTCAG ACAGTTTCCA TCCAGCAGAC TCTCCTGAGT ACAAAGGGCT TGTTTTTACA 1680
AATCCACATC TGAGGCTCAC ATATGGCCTC CCCTCCAGTC CAGAGGGCAT GGAGTTACTA 1740
CCCTTCTCTC TCTGGGCCAA GGTCAGTGTT CTCCAGGCCA GGTAGCTGAT ATAGCTCCTC 1800
TTCCCCAAAG CCTAGCAATG TGCCTCGGAC ATTGGAGGTG CTCAGCATAT GTTTTCTGAT 1860
ACTGACTTAC CAGGAGCATG CAAAACAGCA TGCCAGTAAC ACTGCTATTT CCCTGGTATG 1920
AGCAGACAAG GAGGTTCCCA ACCCACGGTG CTTTGGGGGA AGGTGGTTAT TACCAGCACC 1980
CAAGTCCTTA AATTAGAGTG AATAAATGAA CATTTGGCAA GTCCCTCTTG AAAGCTCGCC 2040
AGCCCCTGAT GTCAGCCACA CAAGTCCAAT CTGTCCTGAG CCAAGGATAC CGATTCAGAG 2100
GCATTTGCTG GGCCCACCCA CTGGGTGCTC TGTGCCATGC CGGGGGCCTG CTCAGGAGAG 2160
ATGAGGACTT AATGAAATCG AAGCCACTCG GAAGATCACC TTTTTCTGGT GAACCTTCAT 2220
GCTGGTGGAA CCAGCAGGGC TCAGATGCAA TTTAGACAGT CTCCTTTCCC TCATTTCCTA 2280
TCATATATCT TTCTCCAAAG AACTGGAGCA AGGGGGAAAG CTGGGGTTTT GTGCTTTCTG 2340
ACTGTTTAAT AATCTGGCTC 2360
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